NM_000579.4:c.477G>A

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  2. NM_000579.4:c.477G>A

HGVS Expressions

  • NG_012637.1:g.8238G>A
  • NM_000579.4:c.477G>A
  • NP_000570.1:p.Ala159=
  • NC_000003.12:g.46373379G>A

Associated Genes

Chemokine, CC Motif, Receptor 5
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Substitution

dbSNP

55639502

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
601373.2United Arab Emirates10.00025Uncertain SignificanceAl-Jaberi et al. 2013 Healthy adult carrier. In this study, on...
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Contributors

  • Asha Deepthi: 04.04.2022

Edit History

  • Asha Deepthi: 04.04.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.